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2-(4-fluorophenyl)-3-phenylquinoline is a complex organic compound with the molecular formula C23H16FN. It is characterized by a quinoline ring system, which is a tricyclic, nitrogen-containing structure. The molecule features a 4-fluorophenyl group attached at the 2-position and a phenyl group at the 3-position, both of which are aromatic rings that contribute to the compound's structure and properties. This chemical is primarily used in the field of medicinal chemistry, particularly in the synthesis of potential therapeutic agents due to its unique structure and potential interactions with biological targets. The presence of the fluorine atom can significantly influence the compound's reactivity, lipophilicity, and binding affinity, making it an interesting candidate for further exploration in drug development.

361-98-8

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361-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 361-98-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 361-98:
(5*3)+(4*6)+(3*1)+(2*9)+(1*8)=68
68 % 10 = 8
So 361-98-8 is a valid CAS Registry Number.

361-98-8Downstream Products

361-98-8Relevant academic research and scientific papers

A nickel-catalyzed: Anti -carbometallative cyclization of alkyne-azides with organoboronic acids: Synthesis of 2,3-diarylquinolines

Ranjith Kumar, Gadi,Kumar, Ravi,Rajesh, Manda,Sridhar Reddy, Maddi

, p. 759 - 762 (2018/02/06)

An anti-carbonickelative cyclization via reversible alkenylnickel E/Z isomerization of 2-azido phenyl propargyl alcohols with aryl boronic acids is achieved using Ni(acac)2 as the catalyst to access 2,3-diaryl quinolines. It represents a rare example of trapping the vinyl metal intermediate with a nitrogen center, a non-carbon center electrophile.

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